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Calorie restriction alters mitochondrial protein acetylation
Authors:Bjoern Schwer   Mark Eckersdorff   Yu Li   Jeffrey C. Silva  Damian Fermin  Martin V. Kurtev  Cosmas Giallourakis  Michael J. Comb  Frederick W. Alt   David B. Lombard
Affiliation:Program in Cellular and Molecular Medicine, Howard Hughes Medical Institute, The Children's Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02115, USA;
Department of Pathology, University of Michigan, Ann Arbor, MI 48109, USA;
Institute of Gerontology, University of Michigan, Ann Arbor, MI 48109, USA;
Cell Signaling Technology, Danvers, MA 01923, USA;
Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA
Abstract:Calorie restriction (CR) increases lifespan in organisms ranging from budding yeast through mammals. Mitochondrial adaptation represents a key component of the response to CR. Molecular mechanisms underlying this adaptation are largely unknown. Here we show that lysine acetylation of mitochondrial proteins is altered during CR in a tissue-specific fashion. Via large-scale mass spectrometry screening, we identify 72 candidate proteins involved in a variety of metabolic pathways with altered acetylation during CR. Mitochondrial acetylation changes may play an important role in the pro-longevity CR response.
Keywords:calorie restriction    longevity    mass spectrometry    metabolism    mitochondria    sirtuins
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